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GeneBe API Showcase
This page demonstrates how to use the GeneBe API to query variant information. The API provides programmatic access to genomic annotations and variant data.
API presented here should be used for checking single variants. If you want to check many variants at once, please use other API endpoints that you will find in the documentation.
Documentation & Advanced Usage
• Complete API documentation:docs.genebe.net/docs/api/overview/
• Interactive endpoint tester:api.genebe.net/cloud/gb-api-doc/swagger-ui/
• Python client for pandas:pypi.org/project/genebe/
• Java CLI for VCF files:github.com/pstawinski/genebe-cli
• All tools documented at:docs.genebe.net
API Request Examples for Variant: 1-212807763-T-G (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=1&pos=212807763&ref=T&alt=G&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "1",
"pos": 212807763,
"ref": "T",
"alt": "G",
"effect": "missense_variant",
"transcript": "NM_001146171.2",
"consequences": [
{
"aa_ref": "F",
"aa_alt": "C",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TATDN3",
"gene_hgnc_id": 27010,
"hgvs_c": "c.515T>G",
"hgvs_p": "p.Phe172Cys",
"transcript": "NM_001042552.3",
"protein_id": "NP_001036017.1",
"transcript_support_level": null,
"aa_start": 172,
"aa_end": null,
"aa_length": 274,
"cds_start": 515,
"cds_end": null,
"cds_length": 825,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "ENST00000366974.9",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001042552.3"
},
{
"aa_ref": "F",
"aa_alt": "C",
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TATDN3",
"gene_hgnc_id": 27010,
"hgvs_c": "c.515T>G",
"hgvs_p": "p.Phe172Cys",
"transcript": "ENST00000366974.9",
"protein_id": "ENSP00000355941.4",
"transcript_support_level": 1,
"aa_start": 172,
"aa_end": null,
"aa_length": 274,
"cds_start": 515,
"cds_end": null,
"cds_length": 825,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "NM_001042552.3",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000366974.9"
},
{
"aa_ref": "F",
"aa_alt": "C",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TATDN3",
"gene_hgnc_id": 27010,
"hgvs_c": "c.515T>G",
"hgvs_p": "p.Phe172Cys",
"transcript": "ENST00000366973.8",
"protein_id": "ENSP00000355940.4",
"transcript_support_level": 1,
"aa_start": 172,
"aa_end": null,
"aa_length": 273,
"cds_start": 515,
"cds_end": null,
"cds_length": 822,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000366973.8"
},
{
"aa_ref": "F",
"aa_alt": "C",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TATDN3",
"gene_hgnc_id": 27010,
"hgvs_c": "c.515T>G",
"hgvs_p": "p.Phe172Cys",
"transcript": "ENST00000531963.5",
"protein_id": "ENSP00000433755.1",
"transcript_support_level": 1,
"aa_start": 172,
"aa_end": null,
"aa_length": 240,
"cds_start": 515,
"cds_end": null,
"cds_length": 723,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000531963.5"
},
{
"aa_ref": "F",
"aa_alt": "C",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TATDN3",
"gene_hgnc_id": 27010,
"hgvs_c": "c.572T>G",
"hgvs_p": "p.Phe191Cys",
"transcript": "ENST00000950486.1",
"protein_id": "ENSP00000620545.1",
"transcript_support_level": null,
"aa_start": 191,
"aa_end": null,
"aa_length": 292,
"cds_start": 572,
"cds_end": null,
"cds_length": 879,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000950486.1"
},
{
"aa_ref": "F",
"aa_alt": "C",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TATDN3",
"gene_hgnc_id": 27010,
"hgvs_c": "c.533T>G",
"hgvs_p": "p.Phe178Cys",
"transcript": "ENST00000933547.1",
"protein_id": "ENSP00000603606.1",
"transcript_support_level": null,
"aa_start": 178,
"aa_end": null,
"aa_length": 287,
"cds_start": 533,
"cds_end": null,
"cds_length": 864,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000933547.1"
},
{
"aa_ref": "F",
"aa_alt": "C",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TATDN3",
"gene_hgnc_id": 27010,
"hgvs_c": "c.515T>G",
"hgvs_p": "p.Phe172Cys",
"transcript": "NM_001146171.2",
"protein_id": "NP_001139643.1",
"transcript_support_level": null,
"aa_start": 172,
"aa_end": null,
"aa_length": 281,
"cds_start": 515,
"cds_end": null,
"cds_length": 846,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001146171.2"
},
{
"aa_ref": "F",
"aa_alt": "C",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TATDN3",
"gene_hgnc_id": 27010,
"hgvs_c": "c.515T>G",
"hgvs_p": "p.Phe172Cys",
"transcript": "ENST00000532324.5",
"protein_id": "ENSP00000431376.1",
"transcript_support_level": 2,
"aa_start": 172,
"aa_end": null,
"aa_length": 281,
"cds_start": 515,
"cds_end": null,
"cds_length": 846,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000532324.5"
},
{
"aa_ref": "F",
"aa_alt": "C",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TATDN3",
"gene_hgnc_id": 27010,
"hgvs_c": "c.515T>G",
"hgvs_p": "p.Phe172Cys",
"transcript": "NM_001042553.3",
"protein_id": "NP_001036018.1",
"transcript_support_level": null,
"aa_start": 172,
"aa_end": null,
"aa_length": 273,
"cds_start": 515,
"cds_end": null,
"cds_length": 822,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001042553.3"
},
{
"aa_ref": "F",
"aa_alt": "C",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TATDN3",
"gene_hgnc_id": 27010,
"hgvs_c": "c.515T>G",
"hgvs_p": "p.Phe172Cys",
"transcript": "ENST00000883558.1",
"protein_id": "ENSP00000553617.1",
"transcript_support_level": null,
"aa_start": 172,
"aa_end": null,
"aa_length": 272,
"cds_start": 515,
"cds_end": null,
"cds_length": 819,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000883558.1"
},
{
"aa_ref": "F",
"aa_alt": "C",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TATDN3",
"gene_hgnc_id": 27010,
"hgvs_c": "c.482T>G",
"hgvs_p": "p.Phe161Cys",
"transcript": "ENST00000933544.1",
"protein_id": "ENSP00000603603.1",
"transcript_support_level": null,
"aa_start": 161,
"aa_end": null,
"aa_length": 262,
"cds_start": 482,
"cds_end": null,
"cds_length": 789,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000933544.1"
},
{
"aa_ref": "F",
"aa_alt": "C",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TATDN3",
"gene_hgnc_id": 27010,
"hgvs_c": "c.452T>G",
"hgvs_p": "p.Phe151Cys",
"transcript": "ENST00000950484.1",
"protein_id": "ENSP00000620543.1",
"transcript_support_level": null,
"aa_start": 151,
"aa_end": null,
"aa_length": 260,
"cds_start": 452,
"cds_end": null,
"cds_length": 783,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000950484.1"
},
{
"aa_ref": "F",
"aa_alt": "C",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TATDN3",
"gene_hgnc_id": 27010,
"hgvs_c": "c.515T>G",
"hgvs_p": "p.Phe172Cys",
"transcript": "ENST00000933546.1",
"protein_id": "ENSP00000603605.1",
"transcript_support_level": null,
"aa_start": 172,
"aa_end": null,
"aa_length": 255,
"cds_start": 515,
"cds_end": null,
"cds_length": 768,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000933546.1"
},
{
"aa_ref": "F",
"aa_alt": "C",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TATDN3",
"gene_hgnc_id": 27010,
"hgvs_c": "c.452T>G",
"hgvs_p": "p.Phe151Cys",
"transcript": "NM_001146170.2",
"protein_id": "NP_001139642.1",
"transcript_support_level": null,
"aa_start": 151,
"aa_end": null,
"aa_length": 253,
"cds_start": 452,
"cds_end": null,
"cds_length": 762,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001146170.2"
},
{
"aa_ref": "F",
"aa_alt": "C",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TATDN3",
"gene_hgnc_id": 27010,
"hgvs_c": "c.452T>G",
"hgvs_p": "p.Phe151Cys",
"transcript": "ENST00000526641.5",
"protein_id": "ENSP00000434801.1",
"transcript_support_level": 2,
"aa_start": 151,
"aa_end": null,
"aa_length": 253,
"cds_start": 452,
"cds_end": null,
"cds_length": 762,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000526641.5"
},
{
"aa_ref": "F",
"aa_alt": "C",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TATDN3",
"gene_hgnc_id": 27010,
"hgvs_c": "c.452T>G",
"hgvs_p": "p.Phe151Cys",
"transcript": "ENST00000883560.1",
"protein_id": "ENSP00000553619.1",
"transcript_support_level": null,
"aa_start": 151,
"aa_end": null,
"aa_length": 252,
"cds_start": 452,
"cds_end": null,
"cds_length": 759,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000883560.1"
},
{
"aa_ref": "F",
"aa_alt": "C",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TATDN3",
"gene_hgnc_id": 27010,
"hgvs_c": "c.515T>G",
"hgvs_p": "p.Phe172Cys",
"transcript": "ENST00000883559.1",
"protein_id": "ENSP00000553618.1",
"transcript_support_level": null,
"aa_start": 172,
"aa_end": null,
"aa_length": 247,
"cds_start": 515,
"cds_end": null,
"cds_length": 744,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000883559.1"
},
{
"aa_ref": "F",
"aa_alt": "C",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TATDN3",
"gene_hgnc_id": 27010,
"hgvs_c": "c.515T>G",
"hgvs_p": "p.Phe172Cys",
"transcript": "NM_001146169.2",
"protein_id": "NP_001139641.1",
"transcript_support_level": null,
"aa_start": 172,
"aa_end": null,
"aa_length": 240,
"cds_start": 515,
"cds_end": null,
"cds_length": 723,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001146169.2"
},
{
"aa_ref": "F",
"aa_alt": "C",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TATDN3",
"gene_hgnc_id": 27010,
"hgvs_c": "c.452T>G",
"hgvs_p": "p.Phe151Cys",
"transcript": "XM_017000328.3",
"protein_id": "XP_016855817.1",
"transcript_support_level": null,
"aa_start": 151,
"aa_end": null,
"aa_length": 260,
"cds_start": 452,
"cds_end": null,
"cds_length": 783,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_017000328.3"
},
{
"aa_ref": "F",
"aa_alt": "C",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TATDN3",
"gene_hgnc_id": 27010,
"hgvs_c": "c.452T>G",
"hgvs_p": "p.Phe151Cys",
"transcript": "XM_017000329.2",
"protein_id": "XP_016855818.1",
"transcript_support_level": null,
"aa_start": 151,
"aa_end": null,
"aa_length": 252,
"cds_start": 452,
"cds_end": null,
"cds_length": 759,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_017000329.2"
},
{
"aa_ref": "F",
"aa_alt": "C",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TATDN3",
"gene_hgnc_id": 27010,
"hgvs_c": "c.515T>G",
"hgvs_p": "p.Phe172Cys",
"transcript": "XM_017000330.3",
"protein_id": "XP_016855819.1",
"transcript_support_level": null,
"aa_start": 172,
"aa_end": null,
"aa_length": 247,
"cds_start": 515,
"cds_end": null,
"cds_length": 744,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_017000330.3"
},
{
"aa_ref": "F",
"aa_alt": "C",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TATDN3",
"gene_hgnc_id": 27010,
"hgvs_c": "c.359T>G",
"hgvs_p": "p.Phe120Cys",
"transcript": "XM_024453283.2",
"protein_id": "XP_024309051.1",
"transcript_support_level": null,
"aa_start": 120,
"aa_end": null,
"aa_length": 221,
"cds_start": 359,
"cds_end": null,
"cds_length": 666,
"cdna_start": null,
"cdna_end": null,
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}
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}